Bronchial Asthma Pathophysiology and management
Transcript of Bronchial Asthma Pathophysiology and management
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Bronchial AsthmaPathophysiology and management
Dr Deepak AggarwalMD, FCCP
Asst. ProfessorPulmonary medicine
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What is Asthma…..Definition ( GINA)
• Asthma is – A chronic inflammatory disorder of the airways in which many cells and cellular elements play a role.
– The chronic inflammation is associated with airway hyper‐responsiveness that leads to recurrent episodes of wheezing , breathlessness, chest tightness and coughing particularly at night or early morning.
– These episodes are usually associated with widespread, but variable airflow obstruction within the lung that is often reversible either spontaneously or with treatment
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Causes/ Risk factors
ENVIRONMENTAL RISK FACTORS
GENETIC SUSCEPTIBILITY ANDGENE‐ENVIRONMENT INTERACTIONS
Perinatal FactorsIndoor and Outdoor AllergensSmoking and Environmental Tobacco SmokeOther PollutantsRace/Ethnicity and Socioeconomic StatusObesityRespiratory Illnesses
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How Asthma develops…..
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PATHOGENESIS
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PATHOGENESIS
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ASTHMA ‐ PATHOPHYSIOLOGY
Asthma
Genetic predispositionIntrinsic vulnerabilityAtopy/allergy
Inflammation underlies disease processes
Phenotype varies by individual and over time
Clinical symptoms also vary by individual and over time
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PATHOLOGY
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Asthma: Pathological changes
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Pathology and consequences
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COPDNeutrophils
No airway hyperresponsiveness
Less bronchodilatorresponse
Limited steroidresponse
Wheezy bronchitis 10%
AsthmaEosinophils
Airway hyperresponsiveness
Bronchodilatorresponse
Steroidresponse
CD4+ T-lymphocytes CD8+ T-lymphocytes
Completelyreversible
incompletelyirreversible
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Physiologic Differences
Asthma• Normal DLCO
• Normal lung volume
• Normal elastic recoil
COPD• Abnormal DLCO
• Hyperinflation
• Decreased elastic recoil
Sciurba FC, CHEST 2004;117S‐124S
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Reversible airflow obstruction + ++ +
Airway inflammation + + + + +
Mucus hypersecretion + + + +
Goblet cell metaplasia + + +
Impaired mucus clearance + + + +
Epithelial damage ++ —
Alveolar destruction — ++
Smooth muscle hypertrophy + + —
Basement membrane thickening +++ —
Disease Pathology Asthma COPD
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Asthma‐Classic presentation
• Intermittent episodic, acute/subacute onset• Breathlessness/chest tightness usually with wheeze
• Cough nocturnal or early morning.• Diurnal and seasonal variation• History of atopy, family history • Polyphonic wheeze, prolonged expiration• However, the examination can be normal.
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Differential diagnosis
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DIAGNOSIS
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Cough, wheezing and
Breathlessness
Minimal or no expectorationAssociated chest tightness
Expectoration mucoid or
mucopurulent
Associated fever, chest pain,
constitutional symptoms
Symptoms variable,Intermittent, recurrent, seasonal, worse at night and provoked by triggers
History of atopy in self or atopy/eczema in family
Symptoms chronic/ progressive/persistent
SUSPECT OTHER DIAGNOSES OR COMPLICATIONS
History of smoking (active or ETS exposure)
Breath Sound intensity normalProminent rhonchi – bilateral, diffuse, polyphonic, expiratory
MANAGE AS ASTHMA
Hyperinflation, pursed lip breathing, diminished
intensity of breath soundsLocalized signsNormal
SUSPECT OTHER DIAGNOSES OR COMPLICATIONS
Sputum for AFB (x3)
Positive Negative
TUBERCULOSIS(Refer to RNTCP)
MANAGE AS COPD
Referral
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Key indicators for considering a diagnosis of asthma
• Typical history • Intermittent symptoms (reversible)• Association of symptoms to weather changes, dust,
smoke, exercise, viral infection, animals with fur or feathers, house-dust mites, mold, pollen, strong emotional expression (laughing or crying hard), airborne chemicals or dust
• Diurnal variation• Family history• Presence of atopy, allergic rhinitis, skin allergies
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Routine Investigations
• Hemogram including eosinophil count
• Blood gas analysis
• X‐ray chest
• Serum electrolytes (Mg, Na, K)
• Spirometry
• Other test to rule out specific diseases
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Spirometry
• Spirometry measurements (FEV1, FVC, FEV1/FVC) before and after bronchodialator helps determine whether there is airflow obstruction and whether it is reversible over the short term
• (12% in increase in FEV1 and absolute increase in 200ml after 200ug of salbutamol inhalation)
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Spirometry
• Spirometry should be done– at the time of initial assessment– after treatment is initiated and symptoms and peak
expiratory flow (PEF) have been stabilized– at least every 1 to 2 years to assess the
maintenance of airway function
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TREATMENT
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Goals of Asthma Therapy
• Prevent recurrent exacerbations and minimize the need for emergency department visits or hospitalizations
• Maintain (near‐) “normal” pulmonary function
• Maintain normal activity levels (including exercise and other physical activity)
• Provide optimal pharmacotherapy with minimal or no adverse effects
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GINA Levels of Asthma Control
Characteristic Controlled Partly controlled(Any present in any week) Uncontrolled
Daytime symptoms None (2 or less / week)
More than twice / week
3 or more features of partly controlled asthma present in any week
Limitations of activities None Any
Nocturnal symptoms / awakening
None Any
Need for rescue / “reliever” treatment
None (2 or less / week)
More than twice / week
Lung function (PEF or FEV1)
Normal< 80% predicted or
personal best (if known) on any day
Exacerbation None One or more / year 1 in any week
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Levels of prevention
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Asthma drug classification
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What are Controllers?
Control/treat chronic
inflammation
Prevent future attacks
Long term control
Prevent airway remodeling
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What Are Relievers?
‐ Rescue medications to treat acute bronchospasm
‐ Quick relief of symptoms
‐ Used during acute attacks
‐ Action usually lasts 4‐6 hrs
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Methods of Medication Delivery
Metered-dose inhaler (MDI) Spacer/holding chamber/face mask
Dry-powder inhaler (DPI) Nebulizer Oral Medication
Tablets, Liquids
Intravenous Medication IV Corticosteroids, IV Aminophylline
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CONTROLLERSInhaled Corticosteroids
Treatment of choice for long-term control of persistent asthma
Benefits Reduced airway inflammation through topical activity
Decreases airway hyper-responsiveness.
Improve lung function and quality of life
Reduce the frequency of exacerbations
Reduced use of quick-relief medicine
**NEVER FOR RESCUE PURPOSES**
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CONTROLLERSCorticosteroids
• Inhaled Beclomethasone Fluticasone Triamcinolone Budesonide Flunisolide
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Anti-inflammatory Effect of Glucocorticoid
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Estimated Comparative Daily Dosages for Adults of Inhaled Corticosteroids
Drug Low DoseStep 2
Medium DoseStep 3
High DoseStep 4
Beclomethasone 1-3 puffs
80 - 240 mcg
3-6 puffs
240 - 480 mcg
>6 puffs
> 480 mcg
Budesonide DPI 1-3 puffs
200 – 600 mcg
3-6 puffs
600 – 1,200 mcg
> 6 puffs
> 600 mcg
Flunisolide 2-4 puffs
500–1,000 mcg
4-8 puffs
1,000–2,000 mcg
> 8 puffs
> 2,000 mcg
Fluticasone 2-6 puffs (44)
88-264 mcg
2-6 puffs (110)
264-660 mcg
> 6 puffs (110)
> 660 mcg
Triamcinolone 4-10 puffs
400-1,000 mcg
10-20 puffs
1,000–2,000 mcg
> 20 puff
> 2,000 mcg
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Corticosteroid Side Effects
Inhaled Local
• Dysphonia
• Cough/throat irritation
• Thrush
• Impaired growth (high dose)?
Systemic (oral, IV)• Fluid retention• Muscle weakness• Ulcers• Malaise• Impaired wound healing• Nausea/Vomiting, HA• Osteoporosis (adults)• Cataracts (adults)• Glaucoma (adults)
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CONTROLLERSLong-acting Beta2-agonists
Salmeterol, Formoterol Indication: Daily long-term control
Advantages Blunt exercise induced symptoms for longer time
Decrease nocturnal symptoms
Improve quality of life
Combination therapy beneficial when added to inhaled corticosteroids
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CONTROLLERSLong-acting Beta2-agonists
NOT for acute symptoms or exacerbations
Onset of effect 30 minutes
Peak effect 1-2 hours
Duration of effect up to 12 hours
NOT a substitute for anti-inflammatory therapy
NOT appropriate for monotherapy
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Useful Beta Adrenergic Effects
• Relax bronchial smooth muscle
• Inhibit mediator release from mast cells, eosinophils, macrophages
• Decrease mucous secretion (submucosal gl)
• Increase mucociliary transport
• Inhibit bronchial oedema
• Inhibit cholinergic transmisssion
• Decrease airway hyperresponsiveness
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CONTROLLERSLeukotriene Modifiers
Cysteinyl Leukotriene Receptor Antagonists Montelukast – Once a day dose Zafirlukast – Twice daily – Empty Stomach
5-Lipoxygenase inhibitors Zileuton – Four times daily
Many drug interactions
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Add‐on ControllersLeukotriene Modifiers
Montelukast
– Improves lung function and asthma control– May protect against exercise induced bronchoconstriction– Not as effective as inhaled corticosteroids– No food restrictions
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RELIEVERSShort-Acting Beta -agonist
• Salbutamol• Terbutaline• levosalbutamol
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RELIEVERSShort-Acting Beta2-Agonists
Most effective medication for relief of acute bronchospasm
Increased need for these medications indicates uncontrolled asthma (and inflammation)
Use “as needed” as regular use
May lower effectiveness
May increase airway hyperresponsiveness
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RELIEVERSShort-Acting Beta2-Agonists
Side Effects:
Increased Heart Rate
Palpitations
Nervousness
Sleeplessness
Headache
Tremor
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Unwanted Beta Adrenergic Effects
• Hypokalemia (K shift into muscle tissue)
• Hyperglycemia (glycogenolysis)
• Hypoxia (pulmonary vasodilation causing increased ventilation/perfusion mismatch)
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Oral Steroid Short Course
• Prednisone 30‐40mg x 10‐14 days for acute exacerbation of Asthma
• no weaning of dose unless long term use
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Step 1 Treatment for Adults and Children > 5: Mild Intermittent
Controller – Daily
‐ Not needed
Reliever – Quick Relief
‐Short‐acting inhaled beta2‐agonist
‐ Increasing use, or use more than 2x/week, may indicate need for long‐term‐control therapy‐
STEP 1
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Step 2 Treatment for Adults and Children > 5: Mild Persistent
STEP 2
Controller – Preferred Daily
‐ Low dose inhaled corticosteroid
Alternatives
‐ leukotriene modifier, OR
‐ Sustained‐release theophylline
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Step 3 Treatment for Adults andChildren > 5: Moderate Persistent
Controller – Preferred Daily
‐ Low to medium dose inhaled corticosteroid (medium dose) and long‐acting beta2‐agonist
Alternatives
‐ Increase inhaled corticosteroids to medium‐
dose range
OR
‐ Low to medium dose inhaled corticosteroid
(medium dose) and either leukotriene
modifier or theophylline
STEP 3
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Step 3 Treatment for Adults andChildren > 5: Moderate Persistent(patients with recurring severe exacerbations)
Controller
‐Medium dose inhaled corticosteroid
(medium dose) and long‐acting beta2‐
agonist
Alternatives
‐ Medium dose inhaled corticosteroid
(medium dose) and either leukotriene
modifier or theophylline
‐ High dose inhaled corticosteroid
‐ Consider referral to a specialist
STEP 4
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Step 4 Treatment for Adults andChildren > 5: Severe Persistent
Controller – Daily
‐ High‐dose inhaled corticosteroid AND‐ Long‐acting inhaled beta2‐agonist AND, if needed,
‐Add leukotriene antagonists & theophylline
‐ Corticosteroid tablets
STEP 5
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Monitor Asthma Control
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Treating to Maintain Asthma Control
Stepping down treatment when asthma is controlled
When controlled on medium‐ to high‐dose inhaled glucocorticosteroids: 50% dose reduction at 3 month intervals (Evidence B)
When controlled on low‐dose inhaled glucocorticosteroids: switch to once‐daily dosing (Evidence A)
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Treating to Maintain Asthma Control
Stepping up treatment in response to loss of control
Rapid‐onset, short‐acting or long‐acting inhaled β2‐agonist bronchodilators provide temporary relief
Need for repeated dosing over more than one/two days signals need for possible increase in controller therapy
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As soon as good control:
• Reduce oral steroids first, then stop
• Reduce relievers before controllers
When good control for 3+ months:
• Reduce inhaled steroids
Managing the well controlled patient
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Therapy to avoid!
• Sedatives & hypnotics• Cough syrups• Anti‐histamines• Immunosuppressive drugs• Immunotherapy• Maintenance oral prednisone >10mg/day
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Managing partly/uncontrolled asthma
• Check the inhaler technique• Check adherence and understanding of medication
• Consider aggravation by:– Exposure to triggers/allergens at home or work– Co‐morbid conditions: GI reflux,rhinitis/sinusitis, cardiac problem
– Medications: Beta‐blockers, NSAIDs, Aspirin
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The Asthma Action Plan
• Helps patients/caregivers manage asthma Uses Peak Flows Spells out medication instructions
• Green Zone 80-100% Peak Flow• Yellow Zone 50-80% Peak Flow• Red Zone Below 50% Peak Flow
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Medication Delivery Demonstrations
Breath Actuated Inhalers
Metered Dose Inhalers with Spacer/Holding Chamber
Dry Powder Inhalers
Nebulizers
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pMDIs
Advantages Disadvantages
Small and portable difficult to learn techniqueUnsuitable for children < 5‐6
Quick to use Unsuitable for the elderly, Cold jet may irritate throatLimited amount of drug
delivered per puff
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Spacers and Holding Chambers
A spacer device enhances delivery by decreasing the velocity of the particles and reducing the number of large particles, allowing smaller particles of drug to be inhaled.
A spacer device with a one-way valve, i.e., holding chamber, eliminates the need for the patient to coordinate actuation with inhalation and optimizes drug delivery.
A simple spacer device without a valve requires coordination between inhalation and actuation.
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DPIs
• Generally easier to use• A minimal inspiratory flow rate is necessary to inhale from a DPI; difficult for some pts to use during an exacerbation
• More ecological than MDIs• Storage may be difficult in humid climates
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Nebulizer
Advantages Disadvantages
No Coordination required Cumbersome
Can be used for all ages ExpensiveEffective in severe asthma Noisy
Treatment takes time
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Which inhalation device for which patient?
• Infants and children pMDI+spacer, nebulizer
up 5 y/o
• Children 5‐9 y/o pMDI+spacer, nebulizer, DPI
• Competent older pMDI, DPI
children and adults
• Incompetent older pMDI+spacer, nebulizer
children/adults
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Key Messages
• Asthma is common and can start at any age
• Asthma can be effectively controlled
• Effective asthma management programs include education, objective measures of lung function, environmental control, and pharmacologic therapy.
• A stepwise approach to pharmacologic therapy is recommended.
• The aim is to accomplish the goals of therapy with the least possible medication.
![Page 66: Bronchial Asthma Pathophysiology and management](https://reader033.fdocuments.in/reader033/viewer/2022052318/587769db1a28ab135e8bde4c/html5/thumbnails/66.jpg)
Thank you